chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	8737819	8737820	T	-	41	GENIC	homozygous	47605847
16	8737986	8737987	A	G	33	GENIC	possibly homozygous	47605848
16	8738016	8738017	T	A	35	GENIC	homozygous	47605849
16	8738881	8738882	A	G	42	GENIC	possibly homozygous	47723393
16	8739321	8739322	G	A	35	GENIC	homozygous	47798739
16	8739352	8739353	T	C	51	GENIC	homozygous	47605851
16	8739577	8739578	T	C	39	GENIC	homozygous	47605852
16	8741270	8741271	A	T	37	GENIC	homozygous	47261958
16	8743366	8743367	T	C	31	GENIC	homozygous	47723405
16	8744161	8744162	T	C	43	GENIC	homozygous	47605855
16	8744850	8744851	A	G	31	GENIC	possibly homozygous	47723409
16	8744983	8744984	A	G	34	GENIC	homozygous	47605856
16	8746354	8746355	A	G	27	GENIC	homozygous	47723417
16	8746772	8746773	A	G	36	GENIC	homozygous	47261960
16	8746907	8746908	C	G	32	GENIC	possibly homozygous	47723419
16	8747083	8747084	A	G	33	GENIC	homozygous	47798740
16	8747484	8747485	A	G	27	GENIC	homozygous	47723421
16	8747837	8747838	G	A	32	GENIC	possibly homozygous	47798741
16	8747915	8747916	A	G	35	GENIC	homozygous	47723431
16	8748136	8748137	T	G	32	GENIC	homozygous	47798742
16	8748255	8748256	T	C	51	GENIC	homozygous	47261962
16	8748524	8748525	G	GTC	11	GENIC	homozygous	47605859
16	8748527	8748528	T	TATCAC	12	GENIC	homozygous	47605860
16	8749348	8749351	AAA	---	21	GENIC	homozygous	47605862
16	8750133	8750134	T	A	52	GENIC	possibly homozygous	47261975
16	8750491	8750492	G	A	38	GENIC	homozygous	47798743
16	8750542	8750543	G	GA	27	GENIC	homozygous	47261977
16	8750547	8750548	T	-	27	GENIC	homozygous	47261979
16	8750600	8750601	C	G	14	GENIC	homozygous	47261981
16	8750974	8750976	AA	--	14	GENIC	heterozygous	47261983
16	8750975	8750976	A	-	14	GENIC	possibly homozygous	47798744
16	8751345	8751346	A	AATAG	6	GENIC	homozygous	47261987
16	8751602	8751603	C	A	35	GENIC	possibly homozygous	47605863
16	8751609	8751610	G	GA	23	GENIC	possibly homozygous	47723453